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233013

Sigma-Aldrich

2-(3-Chlorophenoxy)propionic acid

98%

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About This Item

Linear Formula:
CH3CH(OC6H4Cl)CO2H
CAS Number:
Molecular Weight:
200.62
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

mp

113-115 °C (lit.)

functional group

carboxylic acid
chloro

SMILES string

CC(Oc1cccc(Cl)c1)C(O)=O

InChI

1S/C9H9ClO3/c1-6(9(11)12)13-8-4-2-3-7(10)5-8/h2-6H,1H3,(H,11,12)

InChI key

YNTJKQDWYXUTLZ-UHFFFAOYSA-N

General description

2-(3-Chlorophenoxy)propionic acid is a chiral phenoxy acid herbicide. Enantiomeric resolution of 2-(3-chlorophenoxy)propionic acid has been performed by electrokinetic chromatography using a cyclodextrin as chiral pseudophase (CD-EKC).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Y Martín-Biosca et al.
Electrophoresis, 22(15), 3216-3225 (2001-10-09)
The enantiomeric resolution of chiral phenoxy acid herbicides was performed by electrokinetic chromatography using a cyclodextrin as chiral pseudophase (CD-EKC). A systematic evaluation of several neutral and charged cyclodextrins was made. Among the cyclodextrins tested, (2-hydroxy)propyl beta-cyclodextrin (HP-beta-CD) was found
Iza Matarashvili et al.
Journal of chromatography. A, 1483, 86-92 (2017-01-04)
When polysaccharide-based chiral columns are used in combination with aqueous-organic mobile phases for the separation of enantiomers in high-performance liquid chromatography the separation mode is commonly called "reversed-phase" in analogy to achiral separations. In several earlier and recent studies on

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